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Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2.This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, and the decaffeination process of tea and coffee.
141-43-5: 0152: Ethanolamine: 75 mg/m 3: 30 ppm: 141435: 110-80-5: 0060: 2-Ethoxyethanol: 1845 mg/m 3: 500 ppm: 110805: 111-15-9: 0364: 2-Ethoxyethyl acetate: 2705 mg/m 3: 500 ppm: 111159: 141-78-6: 0367: Ethyl acetate: 7200 mg/m 3: 2000 ppm: 141786 (10% Lower explosive limit LEL) 140-88-5: 0267: Ethyl acrylate: 1227 mg/m 3: 500 ppm: 140885 ...
for Ethyl Acetate/Acetic acid [3] P = 740 mmHg BP Temp. °C % by mole C 4 H 8 O 2; liquid vapor 117.07: 0.0: ... 78.3 75.6: 90.8: 82.3 76.1: 93.2: 86.8 76.4: 94.2: 88 ...
At large scale, ethyl acetoacetate is industrially produced by treatment of diketene with ethanol. [2] The small scale preparation of ethyl acetoacetate is a classic laboratory procedure. [3] It involves Claisen condensation of ethyl acetate. Two moles of ethyl acetate condense to form one mole each of ethyl acetoacetate and ethanol. [4]
acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...
C 4 H 6: methylenecyclopropane: 6142-73-0 C 4 H 6 Br 2 O 2: ethyl dibromoacetate: 617-33-4 C 4 H 6 MgO 4: magnesium acetate: 142-72-3 C 4 H 6 N 2 O 2: dihydrouracil: 504-07-4 C 4 H 6 N 2 O 2: dimethylfurazan monoxide: 2518-42-5 C 4 H 6 N 2 O 2: ethyl diazoacetate: 623-73-4 C 4 H 6 N 2 S: methimazole: 60-56-0 C 4 H 6 N 4 O 2: glycoluril: 496-46 ...